Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Mucopolysaccharidosis type 2, attenuated form
X-linked recessive
Childhood
Mucopolysaccharidosis type 2, severe form
X-linked recessive
Childhood
Mucopolysaccharidosis type 3
Autosomal recessive
Childhood
Mucopolysaccharidosis type 4
Autosomal recessive
Childhood, Infancy
Mucopolysaccharidosis type 4A
Autosomal recessive
Childhood
Mucopolysaccharidosis type 4B
Autosomal recessive
Mucopolysaccharidosis type 6
Autosomal recessive
Childhood
Mucopolysaccharidosis type 6, rapidly progressing
Autosomal recessive
Mucopolysaccharidosis type 6, slowly progressing
Autosomal recessive
Mucopolysaccharidosis type 7
Autosomal recessive
Adolescent, Antenatal, Childhood, Infancy, Neonatal
Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders
Autosomal recessive
Infancy
Mucous membrane pemphigoid
Not applicable
Adolescent, Adult, Childhood, Elderly, Infancy
Mueller-Weiss syndrome
Adult
Muenke syndrome
Autosomal dominant
Antenatal, Neonatal
Mulibrey nanism
Autosomal recessive
Antenatal, Childhood, Infancy, Neonatal
Multicentric carpo-tarsal osteolysis with or without nephropathy
Autosomal dominant
Childhood
Multicentric osteolysis-nodulosis-arthropathy spectrum
Autosomal recessive
Childhood, Infancy
Multicentric reticulohistiocytosis
Not applicable
Adult
Multicystic dysplastic kidney
Not applicable
Infancy, Neonatal
Multifocal atrial tachycardia
Not applicable
Infancy, Neonatal
Multifocal infantile hemangioma with extracutenous involvement
Not applicable
Neonatal
Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome
Not applicable
Infancy, Neonatal
Multifocal motor neuropathy
Unknown
Adult
Multifocal pattern dystrophy simulating fundus flavimaculatus
Autosomal dominant
Adult